All diseases

OMIM ID
263200
OMIM term:
POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE; ARPKD
Alternative terms:
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1
POLYCYSTIC KIDNEY DISEASE, INFANTILE, TYPE I
PKD3, FORMERLY HEPATIC FIBROSIS, CONGENITAL, INCLUDED
CAROLI DISEASE, INCLUDED
(∗) Location:
6p12.3-p12.2  
(†) Associated OMIM genes:
PKHD1  
(‡) Associated MGI genes:
Arl3   Bicc1   Cys1   Ift88   Nek1   Nek8   Pkhd1  

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